American professional soccer club in Hartford, Connecticut.
Fire department in Honolulu, Hawaii.
1CD1 female mice were acutely fed a standard breeding chow or HFD.
2Results: HFD supplements did not alter total caloric intake or body weight.
3HFD mice presented inhibition of cardiac autophagy and displayed increased ischemic injury.
4Conclusions: PPARa mediated weight gain of HFD-treated mice exposed to night neon light.
5Relative mitochondrial content increased, but respiratory efficiency declined by 32 weeks of HFD.
6No difference in food intake was observed between vehicle- and LFE-treated HFD mice.
7The present study investigated the neuroprotective effects of pistachio intake in HFD mice.
8In particular, we found that RES significantly improved memory deficit in HFD-fed mice.
9Exenatide notably decreased the liver weight and hepatic steatosis induced by HFD challenge.
10PC treatment significantly decreased HFD-induced liver weight and hepatic lipid accumulation.
11Activation of HIF ameliorates multiple obesity-related consequences in mice with HFD.
12This study provides insights into and therapeutic target for the HFD-mediated renal injury.
13Chronic HFD caused a decrease of serum miR-150 in WT mice.
14Additionally, fetal mice from mother feed on HFD showed higher mean body weight.
15The molecular mechanisms underlying USP10-regulated hepatic steatosis were further investigated in HFD-treated mice.
16Muc2 deficiency protected mice from HFD-induced fatty liver disease and obesity.